ClinVar Miner

List of variants in gene PTEN reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NM_000314.7(PTEN):c.*10T>A rs769236743
NM_000314.7(PTEN):c.-246C>T rs886047393
NM_000314.7(PTEN):c.1008C>T (p.Tyr336=) rs786201816
NM_000314.7(PTEN):c.1026+121C>T rs536465299
NM_000314.7(PTEN):c.1041C>T (p.Phe347=) rs1554826029
NM_000314.7(PTEN):c.1062G>A (p.Pro354=) rs786202751
NM_000314.7(PTEN):c.1092T>C (p.Ser364=) rs1355576298
NM_000314.7(PTEN):c.1137T>C (p.Tyr379=) rs1295420243
NM_000314.7(PTEN):c.1197A>G (p.Gln399=) rs374684043
NM_000314.7(PTEN):c.132C>T (p.Gly44=) rs150651961
NM_000314.7(PTEN):c.165-9T>G rs878853934
NM_000314.7(PTEN):c.209+10T>C rs770451470
NM_000314.7(PTEN):c.209+7A>G rs1554897284
NM_000314.7(PTEN):c.210-12C>T rs766570103
NM_000314.7(PTEN):c.210-5T>C rs863224358
NM_000314.7(PTEN):c.231C>T (p.Asp77=) rs755953294
NM_000314.7(PTEN):c.234C>A (p.Thr78=) rs35917308
NM_000314.7(PTEN):c.342A>G (p.Glu114=) rs1589646244
NM_000314.7(PTEN):c.426G>C (p.Arg142=) rs878853939
NM_000314.7(PTEN):c.42G>A (p.Arg14=) rs1064794513
NM_000314.7(PTEN):c.493-7C>T rs1554900492
NM_000314.7(PTEN):c.66C>T (p.Asp22=) rs786201335
NM_000314.7(PTEN):c.711G>A (p.Lys237=) rs773353820
NM_000314.7(PTEN):c.741A>G (p.Leu247=) rs1554825217
NM_000314.7(PTEN):c.747G>A (p.Val249=) rs1060503840
NM_000314.7(PTEN):c.774C>T (p.Phe258=) rs1554825246
NM_000314.7(PTEN):c.780A>G (p.Lys260=) rs876658720
NM_000314.7(PTEN):c.783G>A (p.Gln261=) rs760146269
NM_000314.7(PTEN):c.80-6A>G rs1554893744
NM_000314.7(PTEN):c.80-8del rs1060503844
NM_000314.7(PTEN):c.802-2dup rs1554825500
NM_000314.7(PTEN):c.843A>G (p.Pro281=) rs1554825518
NM_000314.7(PTEN):c.855A>G (p.Glu285=) rs751888926
NM_000314.7(PTEN):c.876T>C (p.Asn292=) rs864622098
NM_000314.7(PTEN):c.909T>A (p.Ile303=) rs878853945
NM_000314.8(PTEN):c.1003C>A (p.Arg335=) rs121909231
NM_000314.8(PTEN):c.1026+7T>A rs1589666333
NM_000314.8(PTEN):c.117A>C (p.Ala39=) rs1223327870
NM_000314.8(PTEN):c.129A>G (p.Glu43=) rs1453337737
NM_000314.8(PTEN):c.132C>A (p.Gly44=) rs150651961
NM_000314.8(PTEN):c.135A>G (p.Val45=) rs959491852
NM_000314.8(PTEN):c.164+7A>G rs1589617432
NM_000314.8(PTEN):c.210-4T>C rs1589644668
NM_000314.8(PTEN):c.210-7_210-3del rs587780544
NM_000314.8(PTEN):c.235G>A (p.Ala79Thr) rs202004587
NM_000314.8(PTEN):c.282C>T (p.Asn94=) rs1589646058
NM_000314.8(PTEN):c.354T>C (p.His118=) rs1564830090
NM_000314.8(PTEN):c.396T>C (p.Gly132=) rs1564830257
NM_000314.8(PTEN):c.423T>C (p.His141=) rs1459569607
NM_000314.8(PTEN):c.45A>G (p.Arg15=) rs1064794096
NM_000314.8(PTEN):c.543G>C (p.Leu181=) rs1589659495
NM_000314.8(PTEN):c.555T>C (p.His185=) rs757799618
NM_000314.8(PTEN):c.567A>G (p.Arg189=) rs1589659570
NM_000314.8(PTEN):c.744T>C (p.Pro248=) rs1589663469
NM_000314.8(PTEN):c.765A>G (p.Val255=) rs1589663555
NM_000314.8(PTEN):c.80-10_80-6del rs1589617099
NM_000314.8(PTEN):c.80-23_85del rs1589617079
NM_000314.8(PTEN):c.802-10T>C rs1270511778
NM_000314.8(PTEN):c.802-4T>C rs753469080
NM_000314.8(PTEN):c.858C>T (p.Thr286=) rs876660443
NM_000314.8(PTEN):c.879A>G (p.Gly293=) rs1060503843

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